Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion type Assertion NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_head.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion description "[Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_provenance.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion evidence source_evidence_curated NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_provenance.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion SIO_000772 15286787 NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_provenance.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion wasDerivedFrom uniprot-20150221 NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_provenance.
- NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_assertion wasGeneratedBy ECO_0000218 NP3859.RAre5RKlmp1GWtJTThRx3Zkn5W0oYMVKJtL5yZJH1oLSI130_provenance.